Reaktion #1991866

ord-3747fe761d8b42afbc783630e18814f4

Reaktionsgleichung

[Al+3].[OH-].[OH-].[OH-]
aluminum hydroxide
N#CC=Cc1ccccc1
cinnamonitrile
CC(C)[CH2][Al+][CH2]C(C)C.[H-]
diisobutylaluminum hydride
Cl
hydrochloric acid
O=CC=Cc1ccccc1
cinnamaldehyde
Ausbeute 63.6%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas then added
  2. 2
    Sonstigeformed
  3. 3
    Sonstigethe organic layer was collected
  4. 4
    Sonstigedried
  5. 5
    workup.DISTILLATIONDistillation of the dried solution under reduced pressure

Vorschrift

To a solution of 8 g cinnamonitrile in 100 ml tetrahydrofuran, was added dropwise 50 ml of a 1.5M toluene solution of diisobutylaluminum hydride with ice cooling, and the resulting mixture was stirred at room temperature for two hours. The reaction mixture was slowly poured to 200 ml ice water, hydrochloric acid was then added to dissolve the aluminum hydroxide formed, and the organic layer was collected and dried. Distillation of the dried solution under reduced pressure gave 5.2 g (yield: 63.6%) of cinnamaldehyde.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04839376uspto-grants-1989_06